@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP348164.RAs9tAKsZproENvccKWVRIP_g8y6pyvt8R3KJbsD50pjw> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP348164.RAs9tAKsZproENvccKWVRIP_g8y6pyvt8R3KJbsD50pjw130_head {
  this: np:hasAssertion dgn-np:NP348164.RAs9tAKsZproENvccKWVRIP_g8y6pyvt8R3KJbsD50pjw130_assertion;
    np:hasProvenance dgn-np:NP348164.RAs9tAKsZproENvccKWVRIP_g8y6pyvt8R3KJbsD50pjw130_provenance;
    np:hasPublicationInfo dgn-np:NP348164.RAs9tAKsZproENvccKWVRIP_g8y6pyvt8R3KJbsD50pjw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP348164.RAs9tAKsZproENvccKWVRIP_g8y6pyvt8R3KJbsD50pjw130_assertion a np:Assertion .
  
  dgn-np:NP348164.RAs9tAKsZproENvccKWVRIP_g8y6pyvt8R3KJbsD50pjw130_provenance a np:Provenance .
  
  dgn-np:NP348164.RAs9tAKsZproENvccKWVRIP_g8y6pyvt8R3KJbsD50pjw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP348164.RAs9tAKsZproENvccKWVRIP_g8y6pyvt8R3KJbsD50pjw130_assertion {
  miriam-gene:1630 a ncit:C16612 .
  
  lld:C0677886 a ncit:C7057 .
  
  dgn-gda:DGN511a9ff9bb9cd2407ac409fc0ed1fc97 sio:SIO_000628 miriam-gene:1630, lld:C0677886;
    a sio:SIO_001121 .
}

dgn-np:NP348164.RAs9tAKsZproENvccKWVRIP_g8y6pyvt8R3KJbsD50pjw130_provenance {
  dgn-np:NP348164.RAs9tAKsZproENvccKWVRIP_g8y6pyvt8R3KJbsD50pjw130_assertion dcterms:description
      "[Thus, we propose that the frequent allelic loss at 18q is because of the effect of multiple genes, and there is at least one as yet unidentified tumor suppressor gene at 18q residing distal to SMAD4, SMAD2, and DCC involved in serous ovarian carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:11438451;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP348164.RAs9tAKsZproENvccKWVRIP_g8y6pyvt8R3KJbsD50pjw130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:00+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetv3.0rdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}